홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Diazomethane → Methyl 4-bromo-2,3,5,6-tetrafluorobenzoate

HRID 1470616
노트
인쇄 미리보기

반응식

HRID 1470616 반응식
[Br:1][C:2]1[C:10]([F:11])=[C:9]([F:12])[C:5]([C:6]([OH:8])=[O:7])=[C:4]([F:13])[C:3]=1[F:14].[N+](=[CH2:17])=[N-]>CO>[CH3:17][O:7][C:6](=[O:8])[C:5]1[C:4]([F:13])=[C:3]([F:14])[C:2]([Br:1])=[C:10]([F:11])[C:9]=1[F:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 9550DiazomethaneHCID 2981734-Bromo-2,3,5,6-tetrafluorobenzoic acid

생성물 1

HCID 46311226Methyl 4-bromo-2,3,5,6-tetrafluorobenzoate수율 85%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 4-bromo-2,3,5,6-tetrafluoro-benzoic acid (20 g, 73.49 mmol) in methanol (20 mL) was added an ethereal solution of diazomethane gas until the starting material is completely consumed. Reaction mixture was then evaporated under reduced pressure. The crude solid obtained was purified by flash column chromatography using 5% ethyl acetate in hexane, to obtain title compound as colorless crystalline solid (18 g, 85%).

후처리

  1. customis completely consumed
  2. customReaction mixture
  3. customwas then evaporated under reduced pressure
  4. customThe crude solid obtained
  5. customwas purified by flash column chromatography

출처 및 근거

ORD 기록
ord-d77135383d1b4b8db240f572ea533946
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09006454B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트